生物加工过程
生物加工過程
생물가공과정
Chinese Journal of Bioprocess Engineering
2015年
5期
31-36
,共6页
冯晨龙%葛人杰%段俐%王丽丽
馮晨龍%葛人傑%段俐%王麗麗
풍신룡%갈인걸%단리%왕려려
拟布氏乳杆菌%定向筛选%甘露醇
擬佈氏乳桿菌%定嚮篩選%甘露醇
의포씨유간균%정향사선%감로순
Lactobacillus parabuchneri%directional screening%mannitol
拟布氏乳杆菌K1( Lactobacillus parabuchneri K1)在厌氧条件下可以有效转化果糖生成甘露醇。但当果糖浓度逐步升高时,菌体生长及甘露醇产生速度减慢。为了提高K1菌株在高浓度果糖条件下的生长及转化速率,设计了定向富集耐渗突变株的实验,采用10 L发酵罐,在高渗条件下连续转接培养,培养过程中果糖质量浓度经4次梯度增加,从270 g/L增加到300 g/L。经55 d传代培养后分离纯化,获得耐渗突变株K2。通过2 L发酵罐验证试验,发现K2菌株在300 g/L果糖条件下,果糖利用速率提高103%,发酵周期缩短46?4%,甘露醇的平均产量达到189 g/L,达到理论转化率的94?0%。
擬佈氏乳桿菌K1( Lactobacillus parabuchneri K1)在厭氧條件下可以有效轉化果糖生成甘露醇。但噹果糖濃度逐步升高時,菌體生長及甘露醇產生速度減慢。為瞭提高K1菌株在高濃度果糖條件下的生長及轉化速率,設計瞭定嚮富集耐滲突變株的實驗,採用10 L髮酵罐,在高滲條件下連續轉接培養,培養過程中果糖質量濃度經4次梯度增加,從270 g/L增加到300 g/L。經55 d傳代培養後分離純化,穫得耐滲突變株K2。通過2 L髮酵罐驗證試驗,髮現K2菌株在300 g/L果糖條件下,果糖利用速率提高103%,髮酵週期縮短46?4%,甘露醇的平均產量達到189 g/L,達到理論轉化率的94?0%。
의포씨유간균K1( Lactobacillus parabuchneri K1)재염양조건하가이유효전화과당생성감로순。단당과당농도축보승고시,균체생장급감로순산생속도감만。위료제고K1균주재고농도과당조건하적생장급전화속솔,설계료정향부집내삼돌변주적실험,채용10 L발효관,재고삼조건하련속전접배양,배양과정중과당질량농도경4차제도증가,종270 g/L증가도300 g/L。경55 d전대배양후분리순화,획득내삼돌변주K2。통과2 L발효관험증시험,발현K2균주재300 g/L과당조건하,과당이용속솔제고103%,발효주기축단46?4%,감로순적평균산량체도189 g/L,체도이론전화솔적94?0%。
Lactobacillus parabuchneri K1 can effectively convert fructose to mannitol under anaerobic conditions. However, as fructose concentration increases, cell growth and the yield of mannitol decrease. A directed mutation experiment was designed to improve the cell growth rate and the conversion of L?parabuchneri K1 at high fructose concentration. A 55?day continuous subculture was conducted using a 10?L fermenter with four?time gradient increasing fructose concentration from 270 to ultimate 300 g/L. L?parabuchneri K2, a mutant resistant to high osmotic pressure, increased fructose consumption by 103% in a 2?L fermenter at 300 g/L fructose. Fermentation period was shortened by 46?4% comparing with the K1 strain?The mannitol yield was reached to 189 g/L, 94?0% of theoretical conversion.